Canonical Allele Identifier: CA529002147
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1189155666

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728581_215728582insCACACACACACACA , CM000663.2:g.215728581_215728582insCACACACACACACA GRCh38
NC_000001.10:g.215901923_215901924insCACACACACACACA , CM000663.1:g.215901923_215901924insCACACACACACACA GRCh37
NC_000001.9:g.213968546_213968547insCACACACACACACA NCBI36
NG_009497.1:g.699815_699816insTGTGTGTGTGTGTG
NG_009497.2:g.699867_699868insTGTGTGTGTGTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-198_11712-197insTGTGTGTGTGTGTG MANE Select ENSP00000305941.3:n.11712-198_11712-197insTGTGTGTGTGTGTG
ENST00000674083.1:c.11712-198_11712-197insTGTGTGTGTGTGTG ENSP00000501296.1:n.11712-198_11712-197insTGTGTGTGTGTGTG
ENST00000307340.7:c.11712-198_11712-197insTGTGTGTGTGTGTG ENSP00000305941.3:n.11712-198_11712-197insTGTGTGTGTGTGTG
NM_206933.2:c.11712-198_11712-197insTGTGTGTGTGTGTG NP_996816.2:n.11712-198_11712-197insTGTGTGTGTGTGTG
NM_206933.3:c.11712-198_11712-197insTGTGTGTGTGTGTG NP_996816.2:n.11712-198_11712-197insTGTGTGTGTGTGTG
NM_206933.4:c.11712-198_11712-197insTGTGTGTGTGTGTG MANE Select NP_996816.3:n.11712-198_11712-197insTGTGTGTGTGTGTG